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Development of a species-specific PCR assay for identification of the strictly anaerobic bacterium Selenomonas lacticifex found in biofilm-covered surfaces in brewery bottling halls

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    SYSNO ASEP0506696
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleDevelopment of a species-specific PCR assay for identification of the strictly anaerobic bacterium Selenomonas lacticifex found in biofilm-covered surfaces in brewery bottling halls
    Author(s) Felsberg, Jürgen (MBU-M)
    Jelínková, Markéta (MBU-M)
    Kubizniaková, P. (CZ)
    Matoulková, D. (CZ)
    Source TitleJournal of Applied Microbiology. - : Wiley - ISSN 1364-5072
    Roč. 117, č. 5 (2014), s. 1328-1335
    Number of pages8 s.
    Languageeng - English
    CountryUS - United States
    Keywordsbeer spoilage ; biofilm ; PCR
    Subject RIVEE - Microbiology, Virology
    OECD categoryMicrobiology
    Method of publishingOpen access
    Institutional supportMBU-M - RVO:61388971
    UT WOS000343870700011
    EID SCOPUS84908013133
    DOI10.1111/jam.12610
    AnnotationAimsIn recent years, beer-spoilage cases from strictly anaerobic bacteria have risen in frequency, in connection with the production of non-pasteurized, non-alcohol and low-alcoholic beers and with the lowering of dissolved oxygen in the packaged beer. Selenomonas lacticifex, found in brewer's yeast and in biofilms covering some surfaces in brewery bottling area, is considered to be a beer-spoilage organism. This study aims to develop S.lacticifex-specific PCR assay. The objective of this study was also evaluation of the specificity and reproducibility of the developed PCR assay in real brewery samples.
    Methods and ResultsThree primers (one forward and two reverse) were designed for identification of the strictly anaerobic bacterium S.lacticifex on the basis of the species-specific sequences of the 16S rDNA region. The specificity of the primers was tested against 44 brewery-related non-target micro-organisms that could potentially occur in the same brewery specimens. None of the primer pairs amplified DNA from any of the non-S.lacticifex strains tested including genera from the same family (Pectinatus, Megasphaera, Zymophilus) and the closely related species Selenomonas ruminantium, showing thus 100% specificity.
    ConclusionsThe PCR assay developed in this study enables the detection of the strictly anaerobic bacterium S.lacticifex in real brewery samples including pitching yeast.
    Significance and Impact of the StudySelenomonas lacticifex-specific PCR assay developed in this study allows for the extension of the spectra of detected beer-spoilage micro-organisms in brewing laboratories and thus lowering the risk of contamination of the final product.
    WorkplaceInstitute of Microbiology
    ContactEliška Spurná, eliska.spurna@biomed.cas.cz, Tel.: 241 062 231
    Year of Publishing2020
    Electronic addresshttps://sfamjournals.onlinelibrary.wiley.com/doi/full/10.1111/jam.12610
Number of the records: 1  

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